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dbVar

Database of genomic structural variation

nsv6917101

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:397

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 84 SVs from 18 studies. See in: genome view

Submitted genomic44,105,869-44,106,265

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6917101	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	44,105,869	44,106,265
nsv6917101	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	44,127,419	44,127,815

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18589300	duplication	Sequencing	Split read and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18589300	Submitted genomic		NC_000011.10:g.441 05869_44106265dup	GRCh38 (hg38)		NC_000011.10	Chr11	44,105,869	44,106,265
nssv18589300	Remapped	Perfect	NC_000011.9:g.4412 7419_44127815dup	GRCh37.p13	First Pass	NC_000011.9	Chr11	44,127,419	44,127,815

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv18589300	4e-06	1	242798

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